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A O Wilkie Selected Research

Type B1 Brachydactyly

10/2000Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
8/2000Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
3/2000Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.

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A O Wilkie Research Topics

Disease

4Craniosynostoses (Craniosynostosis)
12/2001 - 03/2000
3Type B1 Brachydactyly
10/2000 - 03/2000
2Acrocephalosyndactylia (Apert Syndrome)
10/2000 - 03/2000
1Osteochondrodysplasias (Spondyloepiphyseal Dysplasia)
07/2001
1Parietal Foramina
01/2001
1Potocki-Shaffer syndrome
01/2001
1Robinow Syndrome
10/2000
1Breech Presentation
08/2000
1Brachydactyly
03/2000
1Craniofacial Dysostosis (Crouzon Disease)
03/2000

Drug/Important Bio-Agent (IBA)

3Receptor Protein-Tyrosine Kinases (Tyrosine Kinase Receptors)IBA
10/2000 - 03/2000
2NucleotidesIBA
12/2001 - 10/2000
2bis(diazo)benzidine (BDB)IBA
10/2000 - 03/2000
1Glycine (Aminoacetic Acid)FDA LinkGeneric
12/2001
1polyglycineIBA
12/2001
1Proteins (Proteins, Gene)FDA Link
07/2001
1DNA (Deoxyribonucleic Acid)IBA
01/2001
1prolylarginineIBA
01/2001
1Transcription Factors (Transcription Factor)IBA
01/2001
1Type 1 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 1)IBA
08/2000
1Type 2 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 2)IBA
03/2000

Therapy/Procedure

1Cesarean Section (Caesarean Section)
08/2000
1Sutures (Suture)
03/2000